Identity
- Trade Name
- velvet XP 250 FDA UDI
- Generic Name
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
- Device Name
- velvet XP250 Nitrile Exam Glove PF, size M FDA UDI
- Model / Reference
- SMTN253 FDA UDI
- Description
- velvet XP250 Nitrile Exam Glove PF, size M FDA UDI
Identifiers
- Catalog Number
- SMTN253 FDA UDI
- Primary DI / UDI-DI
- 00841277108743 FDA UDI
- FDA Product Code
- LZA FDA UDIOPJ FDA UDIQDO FDA UDILZC FDA UDI
- GMDN Term
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6250 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
velvet XP 250 by Sempermed Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Sempermed Usa, Inc.
Sources (1)
- FDA UDI f6d9b7b7-d067-467d-b487-90a6fdb2c294 36 fields · synced Jun 1, 2026